16-HYDROXYHEXADECANOIC ACID

16-HYDROXYHEXADECANOIC ACID Basic information
Product Name:16-HYDROXYHEXADECANOIC ACID
Synonyms:JUNIPERIC ACID;Hexadecanoic acid, 16-hydroxy-;16-HYDROXYHEXADECANOIC ACID;16-HYDROXYPALMITIC ACID;16-hydroxy-hexadecanoicaci;16-Hydroxyhexadecanoic acid, 97+%;16-Hydroxyhexadecanoicacid,98%;16-Hydroxypalmitic acid, Juniperic acid
CAS:506-13-8
MF:C16H32O3
MW:272.42
EINECS:208-028-7
Product Categories:omega-Functional Alkanols, Carboxylic Acids, Amines & Halides;omega-Hydroxycarboxylic Acids;Biochemicals and Reagents;Building Blocks;C13 to C42+;Carbonyl Compounds;Carboxylic Acids;Chemical Synthesis;Fatty Acids and conjugates;Fatty Acyls;Hydroxy Fatty Acids;Lipids;Organic Building Blocks
Mol File:506-13-8.mol
16-HYDROXYHEXADECANOIC ACID Structure
16-HYDROXYHEXADECANOIC ACID Chemical Properties
Melting point 94-98 °C(lit.)
Boiling point 414.4±18.0 °C(Predicted)
density 0.956±0.06 g/cm3(Predicted)
storage temp. 2-8°C
solubility DMF: 20 mg/ml; DMSO: 20 mg/ml; DMSO:PBS(pH 7.2) (1:2): 0.33 mg/ml; Ethanol: 2.5 mg/ml
pka4.78±0.10(Predicted)
form Crystalline Powder
color White
BRN 1783998
InChIInChI=1S/C16H32O3/c17-15-13-11-9-7-5-3-1-2-4-6-8-10-12-14-16(18)19/h17H,1-15H2,(H,18,19)
InChIKeyUGAGPNKCDRTDHP-UHFFFAOYSA-N
SMILESC(O)(=O)CCCCCCCCCCCCCCCO
LogP4.904 (est)
CAS DataBase Reference506-13-8(CAS DataBase Reference)
EPA Substance Registry System16-Hydroxypalmitic acid (506-13-8)
Safety Information
Risk Statements 36/37/38
Safety Statements 22-24/25
WGK Germany 3
TSCA Yes
HS Code 29181998
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
ALFA English
16-HYDROXYHEXADECANOIC ACID Usage And Synthesis
Description16-hydroxy Hexadecanoic acid is a metabolite of the saturated fatty acid palmitic acid (16:0) that has been hydroxylated on its terminal (ω) carbon. It is produced by ω-hydroxylation of palmitic acid by cytochrome P450 in both plants and animals. In plants, it is commonly a component of cutin.
Chemical Propertieswhite crystalline powder
Uses16-Hydroxyhexadecanoic acid was used in the synthesis of dihydroxypalmitic acids. It was also used to induce the expression of two GRP genes of Arabidopsis thaliana, AtGRP5 and AtGRP23.
DefinitionChEBI: A C16 omega-hydroxy fatty acid and key monomer of cutin in the plant cuticle.
5-BETA-CHOLANIC ACID-7-ALPHA, 12-ALPHA-DIOL 3-ALPHA-HYDROXY-6-OXO-5-ALPHA-CHOLAN-24-OIC ACID METHYL ESTER 3-ACETATE DIHYDROOUABAIN DIMETHYL HEXADECANEDIOATE 16-DOXYL-STEARIC ACID Ursodeoxycholic acid Sodium cholate 16-HYDROXYHEXADECANOIC ACID LITHOCHOLIC ACID HEXADECANEDIOIC ACID 20,22-Dihydrodigoxin Sodium deoxycholate Betulinic acid ACETYLLITHOCHOLIC ACID 3-alpha-Ethoxycarbonyl-12-alpha-hydroxy-7-oxocholan-24-oic acid, methy l ester APOCHOLIC ACID 2-ETHYL-2-(15-METHOXY-15-OXOPENTADECYL)-4,4-DIMETHYL-3-OXAZOLIDINYLOXY BETULINIC ACID METHYL ESTER

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